Shga Sample 750k.tar.gz May 2026
fam <- fread("shga_sample.fam", header=F) colnames(fam) <- c("FID", "IID", "PID", "MID", "Sex", "Pheno") print(paste("Samples:", nrow(fam)))
The next steps depend on the nature of the data. If it's genomic data, you might use tools like SAMtools for sequence alignment/map data, or specific software for variant calling. shga sample 750k.tar.gz
# Example command for inspecting a FASTQ file (common in genomics)
zcat sample.fastq.gz | head
tar -xvzf shga_sample_750k.tar.gz
This will likely produce files like:
Check contents:
tar -tzf shga_sample_750k.tar.gz | head -20
Common contents for a file named like this: fam <- fread("shga_sample